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Obesimed Forte 126 c

EUDAMED

Class IIa (EU MDR)

Ref 029023

by PK Benelux BV

Identity

Trade Name
Obesimed Forte 126 c EUDAMED
Device Name
Obesimed Forte EUDAMED
Model / Reference
029023 EUDAMED

Identifiers

Primary DI / UDI-DI
D-029023MQ EUDAMED
Basic UDI-DI
B-029023MQ EUDAMED
EMDN Code
G0402 ORALLY ADMINISTERED DEVICES FOR APPETITE CONTROL AND REDUCTION OF INTESTINAL ABSORPTION EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Obesimed Forte 126 c by PK Benelux BV — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
PK Benelux BV
EUDAMED SRN
NL-MF-000006672

Sources (1)

  • EUDAMED 8a82fc61-a1b8-4f5b-b45e-c87bfdd922ce 61 fields · synced Jun 17, 2026